United States · FDA National Drug Code directory
SUCRALFATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72189-234_2c285743-2fa6-4132-e063-6294a90adaff
- Product NDC
- 72189-234
- Form
- TABLET
- Composition / generic term
- SUCRALFATE
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210618
- Source listing expiry
- 20261231
Source-listed ingredients
- SUCRALFATE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (72189-234-20) · 72189-234-20
- 90 TABLET in 1 BOTTLE (72189-234-90) · 72189-234-90
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →